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MED15-KLHL22 Fusion FISH Probe

The MED15-KLHL22 Fusion FISH Probe is used to confirm a fusion of the MED15 and KLHL22 genes. The fusion of the MED15 and KLHL22 genes has been associated with Head And Neck Squamous Cell Carcinoma . These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.

** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
MED15-KLHL22-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
MED15-KLHL22-20-RERE 20 (40 μL) 200 μL
MED15-KLHL22-20-REOR 20 (40 μL) 200 μL
MED15-KLHL22-20-REGO 20 (40 μL) 200 μL
MED15-KLHL22-20-REGR 20 (40 μL) 200 μL
MED15-KLHL22-20-REAQ 20 (40 μL) 200 μL
MED15-KLHL22-20-ORRE 20 (40 μL) 200 μL
MED15-KLHL22-20-OROR 20 (40 μL) 200 μL
MED15-KLHL22-20-ORGO 20 (40 μL) 200 μL
MED15-KLHL22-20-ORAQ 20 (40 μL) 200 μL
MED15-KLHL22-20-GORE 20 (40 μL) 200 μL
MED15-KLHL22-20-GOOR 20 (40 μL) 200 μL
MED15-KLHL22-20-GOGO 20 (40 μL) 200 μL
MED15-KLHL22-20-GOGR 20 (40 μL) 200 μL
MED15-KLHL22-20-GOAQ 20 (40 μL) 200 μL
MED15-KLHL22-20-GRRE 20 (40 μL) 200 μL
MED15-KLHL22-20-GROR 20 (40 μL) 200 μL
MED15-KLHL22-20-GRGO 20 (40 μL) 200 μL
MED15-KLHL22-20-GRGR 20 (40 μL) 200 μL
MED15-KLHL22-20-GRAQ 20 (40 μL) 200 μL
MED15-KLHL22-20-AQRE 20 (40 μL) 200 μL
MED15-KLHL22-20-AQOR 20 (40 μL) 200 μL
MED15-KLHL22-20-AQGO 20 (40 μL) 200 μL
MED15-KLHL22-20-AQGR 20 (40 μL) 200 μL
MED15-KLHL22-20-AQAQ 20 (40 μL) 200 μL

MED15 Gene Summary

The protein encoded by this gene is a subunit of the multiprotein complexes PC2 and ARC/DRIP and may function as a transcriptional coactivator in RNA polymerase II transcription. This gene contains stretches of trinucleotide repeats and is located in the chromosome 22 region which is deleted in DiGeorge syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]

Gene Name: Mediator Complex Subunit 15

Chromosome: CHR22: 20861885 -20941919

Locus: 22q11.21

KLHL22 Gene Summary

The Kelch Like Family Member 22 (KLHL22) gene is located on chr22 :20795805-20850170 at 22q11.21.

Gene Name: Kelch Like Family Member 22

Chromosome: CHR22: 20795805 -20850170

Locus: 22q11.21

Gene Diseases

The MED15 KLHL22 Fusion has been associated with the following diseases:

Disease Name
Head And Neck Squamous Cell Carcinoma 

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.